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Genomics of the NF-κB signaling pathway: hypothesized role in ovarian cancer.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Germline mutations in the p73 gene do not predispose to familial prostate-brain cancer.
- Published in:
- Prostate, 2001, v. 48, n. 4, p. 292, doi. 10.1002/pros.1109
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- Publication type:
- Article
Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.
- Published in:
- JNCI Cancer Spectrum, 2021, v. 5, n. 4, p. 1, doi. 10.1093/jncics/pkab044
- By:
- Publication type:
- Article
Rare loss of function variants in candidate genes and risk of colorectal cancer.
- Published in:
- Human Genetics, 2018, v. 137, n. 10, p. 795, doi. 10.1007/s00439-018-1938-4
- By:
- Publication type:
- Article
Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.
- Published in:
- Human Genetics, 2017, v. 136, n. 2, p. 165, doi. 10.1007/s00439-016-1738-7
- By:
- Publication type:
- Article
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
- Published in:
- Human Genetics, 2014, v. 133, n. 1, p. 95, doi. 10.1007/s00439-013-1355-7
- By:
- Publication type:
- Article
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 705, doi. 10.1007/s00439-010-0819-2
- By:
- Publication type:
- Article
TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects.
- Published in:
- Human Genetics, 2007, v. 121, n. 1, p. 65, doi. 10.1007/s00439-006-0289-8
- By:
- Publication type:
- Article
Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia.
- Published in:
- Human Genetics, 2005, v. 117, n. 5, p. 494, doi. 10.1007/s00439-005-1338-4
- By:
- Publication type:
- Article
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 522, doi. 10.1007/s00439-003-1006-5
- By:
- Publication type:
- Article
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 2, p. 38, doi. 10.3390/jpm10020038
- By:
- Publication type:
- Article
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 2, p. 30, doi. 10.3390/jpm10020030
- By:
- Publication type:
- Article
Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01059
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- Publication type:
- Article
Evidence for genetic influences on smoking in adult women twins.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 236, doi. 10.1111/j.1399-0004.1995.tb04303.x
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- Publication type:
- Article
Genetic sex validation for sample tracking in next-generation sequencing clinical testing.
- Published in:
- BMC Research Notes, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13104-024-06723-w
- By:
- Publication type:
- Article
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
- Published in:
- Human Genetics, 2022, v. 141, n. 11, p. 1739, doi. 10.1007/s00439-022-02442-z
- By:
- Publication type:
- Article
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke.
- Published in:
- JAMA Neurology, 2015, v. 72, n. 7, p. 781, doi. 10.1001/jamaneurol.2015.0582
- By:
- Publication type:
- Article
Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease.
- Published in:
- JAMA Neurology, 2014, v. 71, n. 11, p. 1394, doi. 10.1001/jamaneurol.2014.1491
- By:
- Publication type:
- Article
ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants.
- Published in:
- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-016-0391-z
- By:
- Publication type:
- Article
A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Childhood exposures to environmental chemicals and neurodevelopmental outcomes in congenital heart disease.
- Published in:
- PLoS ONE, 2022, v. 17, n. 11, p. 1, doi. 10.1371/journal.pone.0277611
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- Publication type:
- Article
Allocation of Resources to Communication of Research Result Summaries.
- Published in:
- Journal of Empirical Research on Human Research Ethics, 2016, v. 11, n. 4, p. 364, doi. 10.1177/1556264616667126
- By:
- Publication type:
- Article
GLAD YOU ASKED: PARTICIPANTS' OPINIONS OF RE-CONSENT FOR DBGAP DATA SUBMISSION.
- Published in:
- Journal of Empirical Research on Human Research Ethics, 2010, v. 5, n. 3, p. 9, doi. 10.1525/jer.2010.5.3.9
- By:
- Publication type:
- Article
High Density GWAS for LDL Cholesterol in African Americans Using Electronic Medical Records Reveals a Strong Protective Variant in APOE.
- Published in:
- CTS: Clinical & Translational Science, 2012, v. 5, n. 5, p. 394, doi. 10.1111/j.1752-8062.2012.00446.x
- By:
- Publication type:
- Article
Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Dietary fatty acid intake is associated with paraoxonase 1 activity in a cohort-based analysis of 1,548 subjects.
- Published in:
- Lipids in Health & Disease, 2013, v. 12, n. 1, p. 1, doi. 10.1186/1476-511X-12-183
- By:
- Publication type:
- Article
Harmonizing variant classification for return of results in the All of Us Research Program.
- Published in:
- Human Mutation, 2022, v. 43, n. 8, p. 1114, doi. 10.1002/humu.24317
- By:
- Publication type:
- Article
47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations.
- Published in:
- 2024
- By:
- Publication type:
- Abstract
A case for expanding carrier testing to include actionable X‐linked disorders.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Enrichment sampling for a multi-site patient survey using electronic health records and census data.
- Published in:
- 2019
- By:
- Publication type:
- journal article
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
- Published in:
- Journal of the American Medical Informatics Association, 2012, v. 19, n. 2, p. 212, doi. 10.1136/amiajnl-2011-000439
- By:
- Publication type:
- Article
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30678-w
- By:
- Publication type:
- Article
Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0268725
- By:
- Publication type:
- Article
ShareDNA: a smartphone app to facilitate family communication of genetic results.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-020-00864-0
- By:
- Publication type:
- Article
Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 6, p. 700, doi. 10.1002/mgg3.328
- By:
- Publication type:
- Article
Building a family network from genetic testing.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 2, p. 122, doi. 10.1002/mgg3.259
- By:
- Publication type:
- Article
Discordance in selected designee for return of genomic findings in the event of participant death and estate executor.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 2, p. 172, doi. 10.1002/mgg3.274
- By:
- Publication type:
- Article
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.
- Published in:
- Journal of the American Heart Association, 2023, v. 12, n. 5, p. 1, doi. 10.1161/JAHA.121.026561
- By:
- Publication type:
- Article
Concentration of Smaller High-Density Lipoprotein Particle (HDL-P) Is Inversely Correlated With Carotid Intima Media Thickening After Confounder Adjustment: The Multi Ethnic Study of Atherosclerosis (MESA).
- Published in:
- 2016
- By:
- Publication type:
- journal article
HDL-3 is a superior predictor of carotid artery disease in a case-control cohort of 1725 participants.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42427-z
- By:
- Publication type:
- Article
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
- Published in:
- Genetic Epidemiology, 2016, v. 40, n. 6, p. 470, doi. 10.1002/gepi.21976
- By:
- Publication type:
- Article
Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network.
- Published in:
- Genetic Epidemiology, 2015, v. 39, n. 5, p. 376, doi. 10.1002/gepi.21902
- By:
- Publication type:
- Article
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
- Published in:
- Genetic Epidemiology, 2011, v. 35, n. 8, p. 887, doi. 10.1002/gepi.20639
- By:
- Publication type:
- Article
Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels.
- Published in:
- Genetic Epidemiology, 2005, v. 29, n. S1, p. S72, doi. 10.1002/gepi.20112
- By:
- Publication type:
- Article
Linkage analysis of 150 high-risk prostate cancer families at 1q24-25.
- Published in:
- Genetic Epidemiology, 2000, v. 18, n. 3, p. 251, doi. 10.1002/(SICI)1098-2272(200003)18:3<251::AID-GEPI5>3.0.CO;2-X
- By:
- Publication type:
- Article
Preface.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. Sxxxi, doi. 10.1002/gepi.1370170702
- By:
- Publication type:
- Article
Impact of family structure on the power of linkage tests using sib-pair methods.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. S575, doi. 10.1002/gepi.1370170793
- By:
- Publication type:
- Article